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1 erase might be involved in the production of stearate.
2  modified with the fatty acids palmitate and stearate.
3 rporation into the fatty acids palmitate and stearate.
4 l that determines preferential attachment of stearate.
5  location virtually eliminated attachment of stearate.
6 ihydroxy-palmitate and 18-hydroxy-9,10-epoxy-stearate.
7  stearates or a combination of palmitate and stearate.
8 ic transport of a fluorescent fatty acid NBD-stearate.
9  for laurate to a low of 13% of the dose for stearate.
10  activity was greatly stimulated by ascorbyl stearate.
11  activity but were less potent than ascorbyl stearate.
12 nguish among PE, sodium dodecyl sulfate, and stearates.
13 d to form ethoxylated glucam (PEO(n)-glucam) stearates.
14 orescent fatty acid analogue, 12-anthroyloxy stearate (12-AS), between model membrane vesicles.
15 e (16:1n7) from saturated fatty acids (SFA), stearate (18:0) and palmitate (16:0), respectively.
16 m Garcinia mangostana, generates an elevated stearate (18:0) phenotype in transgenic Brassica plants.
17                                 In addition, stearate (18:0) was reduced by 50% in leaves and by 30%
18 ificity for palmitate (16:0)-ACP rather than stearate (18:0)-ACP.
19 of spinach ACP with decanoate (10:0-ACP) and stearate (18:0-ACP) attached to the 4'-phosphopantethein
20 le reduction of oleate contributed little to stearate (2%).
21                    Palmitic acid (29.7%) and stearate (21.3%) are the most common fatty acids.
22 s show that heterogeneous agglomerates of Al-stearate and a Zn-carboxylate complex with Zn-stearate n
23 s through the chemical reaction between zinc stearate and an excess amount of alcohols in hydrocarbon
24  palmitoleate, palmitate, linoleate, oleate, stearate and arachidonate.
25                Thermal decomposition of zinc stearate and gallium nitrate after hot injection of the
26 atty acid R(a) under all conditions, whereas stearate and myristate tracers consistently underestimat
27 palmitoleate, from the saturated fatty acids stearate and palmitate, respectively.
28 d to fatty acids by oxidation over manganese stearate and subsequent processing.
29 B and desT in cells grown in the presence of stearate and their repression when oleate was present.
30 le mutant was unable to desaturate exogenous stearate and was an UFA auxotroph.
31                         It became clear that stearates and sodium dodecyl sulfates can cause substant
32 esized novel iodinated analogs of oleate and stearate, and we showed that heterogeneous S-acylation c
33             Chain elongation of palmitate to stearate appeared to occur in a different compartment.
34                        Furthermore, ascorbyl stearate appears to be a general pleckstrin domain ligan
35                       We identified ascorbyl stearate as a compound that binds to the pleckstrin doma
36  In addition, this paper introduces ascorbyl stearate as a pleckstrin domain ligand that can modulate
37         Ascorbyl palmitate (AP) and ascorbyl stearate (AS) are examples of food additives, which have
38  of vitamin A, retinyl palmitate and retinyl stearate, as well as several minor retinyl esters, in a
39  the carboxylate group of SCP-2 bound [1-13C]stearate at neutral pH; lack of electrostatic interactio
40 parate binding loci if alpha-LA indeed binds stearate at these concentrations.
41 he transmembrane span is the main signal for stearate attachment, but the sequence context and the ce
42  in hepatocytes in response to palmitate and stearate by a proteasome-dependent pathway.
43 t the desaturation of saturated fats such as stearate by SCD is an essential step mediating their ind
44                                              Stearate (C:18) completely inhibited the EGF-induced cel
45 The tsetse vector form requires synthesis of stearate (C18), whereas the bloodstream form needs myris
46 omal beta-oxidation of uniformly 13C-labeled stearate (C18:0) and oleate (C18:1) resulted in chain sh
47 18:1 cis), 9.4; palmitate (C16:0), 16.2; and stearate (C18:0), 21.0.
48  fatty acids, such as palmitic acid (C16:0), stearate (C18:0), or oleate (C18:1), are used in cells t
49 : pH titratability of the SCP-2 bound [1-13C]stearate carboxylate group.
50 ely 35% (P < 0.05) with weight loss, whereas stearate CoA (18:0; -17%; 0.65 +/- 0.05 vs. 0.54 +/- 0.0
51 rtially responsible for determining the high stearate composition of mangosteen seed oil and that Fat
52 nctionalized with lysine and polyoxyethylene stearate conjugate (LPS) to interact with ATB(0,+), an a
53  acylation site had a moderate effect on the stearate content.
54                              Desaturation of stearate contributed 67% of the oleate, while reduction
55                              The increase in stearate correlated with the presence of the ribozyme ge
56 organic excipients such as sucrose, lactose, stearate, dextrin, and starch were also detected.
57 urface: the chemical shift of bound [18-13C]-stearate; dicarboxylic/monocarboxylic acid cis-parinaric
58 of zinc carboxylates are unrelated to the Al-stearate distribution.
59                    However, in Scd1-/- mice, stearate does not induce lipogenesis, and Srebp-1c and P
60 we compared the activity of estradiol-17beta-stearate (E(2)-17beta-S) with that of estradiol-17beta (
61 y faster broadening (DeltaH(pp)) of 16-doxyl-stearate ESR spectrum when compared to glucose syrup cap
62 lene terephthalate, polyisoprene, poly(vinyl stearate), ethylene-vinyl acetate, polyepoxide, paraffin
63  and hepatic glycogen stores are depleted in stearate-fed Scd1-/- mice.
64 -activated protein kinase is also induced by stearate feeding in Scd1-/- mice.
65 cer (as a prodrug therapeutic of niclosamide stearate for i.v. and other administration routes, exemp
66 e increased FABP levels, the fraction of NBD-stearate found in cytosol, and the observed cytoplasmic
67       Pretreatment of cells with 0.15 mmol/L stearate from 0 to 6 hours inhibits, in parallel, both t
68 d salt, it could force the newly formed zinc stearate gradually but completely back onto the existing
69 edium chain triglyceride (MCT) oil, glyceryl stearate (GS) or hydrogenated palm oil (HPO) as compared
70 Oleogels containing 0.1% betaC, 20% glyceryl stearate (GS), with lecithin (L) or hydrogenated lecithi
71                                 In contrast, stearate had little effect on insulin-like growth factor
72       Cells treated with 0.1 mm [U-(13)C(18)]stearate had markedly disparate acetyl-CoA enrichments (
73 fatty acid spin-label, [15N,2H12]-5-nitroxyl stearate, have been obtained at the two sample orientati
74 ds tested, C18 esters, namely hydroxytyrosyl stearate (HtySte) and hydroxytyrosyl oleate (HtyOle), we
75 chidonate, linoleate, oleate, palmitate, and stearate in equilibrium with bovine serum albumin (BSA).
76 d to measure the cytoplasmic movement of NBD-stearate in hepatocytes.
77 rse MnO nanocrystals by simple heating of Mn stearate in octadecene was studied systematically and qu
78                          Chain shortening of stearate in peroxisomes generates acetyl-CoA, which is s
79 the relative concentrations of palmitate and stearate in phosphatidylethanolamine, phosphatidylinosit
80 nocytes, which resulted in increased retinyl stearate in skin of aged Tgfa(-/-) mice.
81 pleted, resulting in elevated levels of free stearate in the gut lumen.
82 able marker gene, was shown to increase leaf stearate in two of 13 maize lines.
83 a confirmed the presence of two disaccharide stearates in the surfactant, which were undetectable by
84 e (and very poorly with [3H]myristate or [3H]stearate) in digitonin-permeabilized cells.
85 angosteen (Garcinia mangostana) stores 18:0 (stearate) in its seed oil in amounts of up to 56% by wei
86 > 0.5), the relative amount of palmitate and stearate increased from 35+/-5 to 44+/-8% and 4+/-1 to 7
87 ediated trait was heritable, as evidenced by stearate increases in the leaves of the R1 plants derive
88 were immediately placed in Ringer's lactate; stearate indicator microelectrodes were placed in tempor
89 e microvoltammetry, used in combination with stearate indicator, Ag-AgCl reference and stainless stee
90 a show that the saturated FFAs palmitate and stearate induced cholangiocyte lipoapoptosis by way of c
91                                Palmitate and stearate induced cholangiocyte lipoapoptosis in a concen
92 strate that the saturated FFAs palmitate and stearate induced robust and rapid cell death in cholangi
93 rget, PUMA, were critical for palmitate- and stearate-induced cholangiocyte lipoapoptosis.
94 w here that a diet high in the saturated fat stearate induces lipogenic genes in wild-type mice, with
95 toplasmic tail of HA contain only palmitate, stearate is exclusively attached to a cysteine positione
96                                         Some stearate is found in crystalline form-identifiable by po
97                           Surprisingly, this stearate labeled near the carboxyl end undergoes more lo
98  titanium vapor deposited onto a C18 cadmium stearate Langmuir-Blodgett monolayer supported on Au, Si
99 s, proved decisive for the formation of zinc stearate-like (ZnSt2) soaps.
100  leaves of the R1 plants derived from a high-stearate line.
101 rotein, in which addition of alpha-LA to the stearate-loaded indicator protein reverses the decrease
102                   In addition, we found that stearate markedly promoted mineralization of CVCs as com
103                                 Therefore, a stearate metabolite derived from lipogenesis might be a
104 5-doxylstearic acid-loaded apo-alpha-LA with stearate (micelles) seem to suggest separate binding loc
105 tly used in the chain elongation of a second stearate molecule to form very long chain fatty acids.
106 n the biotransformation of 8:2 fluorotelomer stearate monoester (8:2 FTS) in aerobic soils was conduc
107 tearate and a Zn-carboxylate complex with Zn-stearate nano-aggregates in proximity are distributed ra
108                 Cytoplasmic transport of NBD-stearate occurred by isotropic diffusion with no evidenc
109 ure of [(13)C]-labeled myristate, palmitate, stearate, oleate, and linoleate was infused in healthy m
110 fed in random order were laurate, palmitate, stearate, oleate, elaidate (the trans isomer of oleate),
111 ry GC cultures with palmitate, palmitoleate, stearate, oleate, linoleate, and alpha-linolenate, repre
112 f different fatty acids methyl esters (FAME: stearate, oleate, linoletate and linolenate) on a mixtur
113                     The inhibitory effect of stearate on cell proliferation was dose and time depende
114 tides were also modified by palmitate and/or stearate on Cys residues.
115 e of multiple concentrations of [U-(13)C(18)]stearate or [U-(13)C(16)] palmitate.
116 azone in HepG2 cells in culture using [U-13C]stearate or [U-13C]oleate and mass isotopomer analysis.
117 own in the presence of 0.7 mmol/liter [U-13C]stearate or [U-13C]oleate, and in the presence and absen
118  Cys residues were acylated by palmitates or stearates or a combination of palmitate and stearate.
119 hates contained long-chain compounds such as stearates or fatty acids, which were falsely identified
120 residues was acylated by either palmitate or stearate, or both Cys residues were acylated by palmitat
121 eate (20% by weight) but not with palmitate, stearate, or linoleate.
122 phatidylcholine molecular species containing stearate paired with a polyunsaturated fatty acid to Ptd
123 ecific LPE acyltransferase that controls the stearate/palmitate homeostasis of PE and the metabolites
124 1 specific acyltransferase that controls the stearate/palmitate ratio of phosphatidylethanolamine (PE
125                                          The stearated peptide blocked the binding of Lyn to the beta
126 (glutamate pool), and in chain elongation of stearate (peroxisomal pool).
127                  The plants with the altered stearate phenotype were shown to express ribozyme RNA.
128 abundant with small amounts of palmitate and stearate, possibly because of the way the fused recombin
129   The biosynthesis of lupeol-3-(3'R-hydroxy)-stearate (procrim b, 1) was investigated in the Mexican
130                      In the absence of SCD1, stearate promotes oxidation, leading to protection from
131 on of sorbitan tristearate (STS) and sucrose stearate (S-370) increased the crystallization speed of
132 ssion by 38% (p = 0.01) and 53% (p = 0.006); stearate similarly decreased expression of PGC-1alpha an
133                                          The stearate spin-labeled at C5 has the highest affinity for
134 ransgenic plants that accumulate 55-68% more stearate than plants expressing the wild-type enzyme.
135 transferase activity and caused a shift from stearate to palmitate species in PE, dimethyl-PE, and ph
136 n addition to introducing a double bond into stearate to produce oleate, performed an additional roun
137                            The peptide was N-stearated to enable cellular internalization.
138 omponents were observed on Teflon and ferric-stearate-treated surfaces.
139 in Brassica seeds led to the accumulation of stearate up to 22% in seed oil.
140 e a study of beta-oxidation of palmitate and stearate using HepG2 cells cultured in the presence of m
141  S83 was spray-dried with lactose and sodium stearate using spray-drying.
142 rences in the fatty acid pattern of HA: more stearate was attached if human viruses were grown in mam
143                                    Exogenous stearate was converted to 18:1Delta9 and supported the g
144  but the saturated fatty acids palmitate and stearate were not effective.

 
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